Genotypic and phenotypic analyses of Korean patients with syndromic craniosynostosis.

Yu, J E; Jeong, S-Y; Yang, J-A; Park, M S; Kim, H J; Yoon, S H

Yu, J E; Jeong, S-Y; Yang, J-A; Park, M S; Kim, H J; Yoon, S H.

Clin Genet ; 76(3): 287-91, 2009 Sep.

Article in En | MEDLINE | ID: mdl-19624690

Subject(s)

Asian People/genetics; Craniosynostoses/genetics; Craniosynostoses/pathology; Abnormalities, Multiple/genetics; Child; Child, Preschool; Craniosynostoses/diagnostic imaging; Female; Genotype; Humans; Infant; Infant, Newborn; Korea; Male; Mutation/genetics; Phenotype; Radiography; Receptor, Fibroblast Growth Factor, Type 2/genetics; Syndrome

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Craniosynostoses / Asian People Type of study: Diagnostic_studies Limits: Child / Child, preschool / Female / Humans / Infant / Male / Newborn Country/Region as subject: Asia Language: En Journal: Clin Genet Year: 2009 Document type: Article Country of publication: Denmark

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